PlainRecalls

Luminex Molecular Diagnostics

Compiled from official public sources by the publisher.

2 recalls on record · Latest: Oct 30, 2019

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Agency notice ledger

Federal filing book Luminex Molecular Diagnosti… LIGHT-BOOK · SINGLE-AGENCY

#5,250 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #5,250 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Devices (2)
  • CAT medical devices
  • CATS 1 category
  • LATEST Oct 30, 2019
  • PHOTO 3M Company

Nearest notice-volume peer: 3M Company (0 notice gap)

Luminex Molecular Diagnostics accounts for about 0.002% of the 104,423-notice archive on 2 distinct filings — a light share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

How Luminex Molecular Diagnosti… compares to 14,151 recalling firms

Luminex Molecular Diagnostics ranks 5,250th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Luminex Molecular Diagnosti… vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

2 5250th of 14151 higher than 8,037 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-14

Luminex Molecular Diagnosti… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Luminex Molecular Diagnostics holds about 0.002% of archive notices alongside 2 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Oct 30, 2019

xTAG Respiratory Viral Panel (RVP): Box Label: xTAG RVP (Respiratory Viral Panel). Catalogue Number:I019C0111 in vitro diagnostic test
FDA Devices Moderate Jun 19, 2019

xTAG Gastrointestinal Pathogen Panel intended for the simultaneous qualitative detection and identification of multiple viral, bacterial and parasitic nucleic acids in human stool specimens or human stool (GPP) Kit, IVD, REF I032C0316.

Luminex Molecular Diagnosti… is a small archive contributor

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

3M Company 2 3M Company/3m Espe Dental Products 2 A.o. Smith Electrical Products Co., of Tipp City, Ohio 2 Abbott GmbH 2

Frequently Asked Questions

How many federal recall notices name Luminex Molecular Diagnosti…? ▼
PlainRecalls indexes 2 distinct federal recall events naming Luminex Molecular Diagnostics, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Luminex Molecular Diagnosti… sit among other recalling firms? ▼
Luminex Molecular Diagnostics ranks #5,250 of 14,151 by distinct recall-event count among 14,151 firms in this archive (57th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Luminex Molecular Diagnosti…'s notices? ▼
FDA Devices accounts for 2 of this firm's 2 indexed notices.
What product category dominates Luminex Molecular Diagnosti…'s filing book? ▼
Filings for Luminex Molecular Diagnostics span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Luminex Molecular Diagnostics: 2 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Luminex Molecular Diagnostics; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026